Abstract
Data in this article is associated with our research article, Electronic Properties of Fe Charge Transfer Complexes – a Combined Experimental and Theoretical Approach [1].The oxidation and reduction potentials of fourteen FeII complexes are presented here, as extracted from the redox data obtained from its associated cyclic voltammograms, which were measured at scan rates varying from 0.05 V.s−1 to 5.00 V.s−1, under similar experimental conditions. Acetonitrile was used as solvent, and tetrabutylammonium hexafluorophosphate as supporting electrolyte. All data are reported versus the FeII redox couple in ferrocene.
Highlights
Data in this article is associated with our research article, Electronic Properties of Fe Charge Transfer Complexes – a Combined Experimental and Theoretical Approach [1]
The oxidation and reduction potentials of fourteen FeII complexes are presented here, as extracted from the redox data obtained from its associated cyclic voltammograms, which were measured at scan rates varying from 0.05 V.s−1 to 5.00 V.s−1, under similar experimental conditions
A 2 mL electrochemical cell was used for all electrochemical analyses of the samples, which consisted of a glassy carbon working electrode, Pt reference electrode and a Pt auxiliary electrode
Summary
Data in this article is associated with our research article, Electronic Properties of Fe Charge Transfer Complexes – a Combined Experimental and Theoretical Approach [1]. Cyclic voltammograms and electrochemical data of FeII polypyridine complexes Jeanet Conradie∗, Karel G. von Eschwege The oxidation and reduction potentials of fourteen FeII complexes are presented here, as extracted from the redox data obtained from its associated cyclic voltammograms, which were measured at scan rates varying from 0.05 V.s−1 to 5.00 V.s−1, under similar experimental conditions.
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